A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy von Penkl, Anja, Reunert, Janine, Debus, Otfried M., Homann, Anna, Och, Ulrike, Rust, Stephan, Marquardt, Thorsten

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Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1 von Thalwitzer, Kim M, Driedger, Jan H, Xian, Julie, Saffari, Afshin, Zacher, Pia, Bölsterli, Bigna K, McKeown Ruggiero, Sarah, Sullivan, Katie Rose, Datta, Alexandre N, Kellinghaus, Christoph, Althaus, Jürgen, Wiemer-Kruel, Adelheid, van Baalen, Andreas, Pampel, Armin, Alber, Michael, Braakman, Hilde M H, Debus, Otfried M, Denecke, Jonas, Hobbiebrunken, Elke, Breitweg, Ina, Diehl, Danielle, Eitel, Hans, Gburek-Augustat, Janina, Preisel, Martin, Schlump, Jan-Ulrich, Laufs, Mirjam, Mammadova, Dilbar, Wurst, Carsten, Prager, Christine, Löhr-Nilles, Christa, Martin, Peter, Garbade, Sven F, Platzer, Konrad, Benkel-Herrenbrueck, Ira, Egler, Kerstin, Fazeli, Walid, Lemke, Johannes R, Runkel, Eva, Klein, Barbara, Linden, Tobias, Schröter, Julian, Steffeck, Heike, Thies, Bastian, von Deimling, Florian, Illsinger, Sabine, Borggraefe, Ingo, Classen, Georg, Wieczorek, Dagmar, Ramantani, Georgia, Koelker, Stefan, Hoffmann, Georg F., Ries, Markus, Helbig, Ingo, Syrbe, Steffen

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Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency von Penkl, Maximilian, Mayr, Johannes A, Feichtinger, René G, Reilmann, Ralf, Debus, Otfried, Fobker, Manfred, Penkl, Anja, Reunert, Janine, Rust, Stephan, Marquardt, Thorsten

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Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: A treatable neurological disorder caused by TPK1 mutations von Banka, Siddharth, de Goede, Christian, Yue, Wyatt W., Morris, Andrew A.M., von Bremen, Beate, Chandler, Kate E., Feichtinger, René G., Hart, Claire, Khan, Nasaim, Lunzer, Verena, Mataković, Lavinija, Marquardt, Thorsten, Makowski, Christine, Prokisch, Holger, Debus, Otfried, Nosaka, Kazuto, Sonwalkar, Hemant, Zimmermann, Franz A., Sperl, Wolfgang, Mayr, Johannes A.

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LIS1 -associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs von Herbst, Saskia M, Proepper, Christiane R, Geis, Tobias, Borggraefe, Ingo, Hahn, Andreas, Debus, Otfried, Haeussler, Martin, von Gersdorff, Gero, Kurlemann, Gerhard, Ensslen, Matthias, Beaud, Nathalie, Budde, Joerg, Gilbert, Michael, Heiming, Ralf, Morgner, Rita, Philippi, Heike, Ross, Sophia, Strobl-Wildemann, Gertrud, Muelleder, Kerstin, Vosschulte, Paul, Morris-Rosendahl, Deborah J, Schuierer, Gerhard, Hehr, Ute

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The Translational Medicine Professional: A Bridge Between Bench and Bedside? von Gohar, Faekah, Gohar, Aisha, Hülskamp, Georg, Debus, Otfried

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Sulthiame in the Primary Therapy of West Syndrome: A Randomized Double‐blind Placebo‐controlled Add‐on Trial on Baseline Pyridoxine Medication von Debus, Otfried Martin, Kurlemann, Gerhard

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The factor V G1691A mutation is a risk for porencephaly: A case-control study von Debus, Otfried M., Kosch, Andrea, Sträter, Ronald, Rossi, Rainer, Nowak-Göttl, Ulrike

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P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG von Fiedler, Barbara J., Debus, Otfried M., Neubauer, Bernd A., Kienle, Matthias, Kurlemann, Gerhard

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Music Therapy Supports Children with Neurological Diseases during Physical Therapy Interventions von Kobus, Susann, Bologna, Franziska, Maucher, Ines, Gruenen, Daniel, Brandt, Ramona, Dercks, Martin, Debus, Otfried, Jouini, Eva

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Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1 von Thalwitzer, Kim M, Driedger, Jan H, Xian, Julie, Saffari, Afshin, Zacher, Pia, Bölsterli, Bigna K, Ruggiero, Sarah McKeown, Sullivan, Katie Rose, Datta, Alexandre N, Kellinghaus, Christoph, Althaus, Jürgen, Wiemer-Kruel, Adelheid, van Baalen, Andreas, Pampel, Armin, Alber, Michael, Braakman, Hilde M H, Debus, Otfried M, Denecke, Jonas, Hobbiebrunken, Elke, Breitweg, Ina, Diehl, Danielle, Eitel, Hans, Gburek-Augustat, Janina, Preisel, Martin, Schlump, Jan-Ulrich, Laufs, Mirjam, Mammadova, Dilbar, Wurst, Carsten, Prager, Christine, Löhr-Nilles, Christa

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Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia von NAMAVAR, Yasmin, BARTH, Peter G, BASEL-VANAGAITE, Lina, EGGENS, Veerle R. C, KRÄGELOH-MANN, Ingeborg, DE MEIRLEIR, Linda, KING, Mary, GRAHAM JR, John M, VON MOERS, Arpad, KNOERS, Nine, SZTRIHA, Laszlo, KORINTHENBERG, Rudolf, KASHER, Paul R, DOBYNS, William B, BAAS, Frank, TIEN POLL-THE, Bwee, VAN RUISSEN, Fred, BROCKMANN, Knut, BERNERT, Günther, WRITZL, Karin, VENTURA, Karen, CHENG, Edith Y, FERRIERO, Donna M

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Early infantile epileptic encephalopathy (Ohtahara syndrome) after maternal electric injury during pregnancy: etiological considerations von Krasemann, Thomas, Hoovey, Secam, Uekoetter, Johannes, Bosse, Henry, Kurlemann, Gerhard, Debus, Otfried M.

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Spontaneous central melatonin secretion and resorption kinetics of exogenous melatonin: a ventricular CSF study von Debus, Otfried M., Lerchl, Alexander, Bothe, Hans W., Bremer, Janbernd, Fiedler, Barbara, Franssen, Meike, Koehring, Jessica, Steils, Michaela, Kurlemann, Gerhard

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Pseudotumor cerebri bei Vakzine-assoziierter ADEM: Eine Liquordruckmessung führt nach Umwegen zur richtigen Diagnose von Klingebiel, Marie-Kristin, Bujupi, Erzen, Debus, Otfried, Endmann, Matthias

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Drug‐Induced Changes in Cerebral Glucose Consumption in Bifrontal Epilepsy von Matheja, Peter, Weckesser, Matthias, Debus, Otfried, Löttgen, Jan, Schuierer, Gerhard, Schober, Otmar, Kurlemann, Gerhard

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Congenital disorder of glycosylation type Id : Clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins von DENECKE, Jonas, KRANZ, Christian, VON KLEIST-RETZOW, Juergen C. H, BOSSE, Kristin, HERKENRATH, Peter, DEBUS, Otfried, HARMS, Erik, MARQUARDT, Thorsten

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Medical Mystery: The Answer: Letter von Kurlemann, Gerhard, Debus, Otfried

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Images in clinical medicine: A medical mystery von Kurlemann, Gerhard, Debus, Otfried

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Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly von Debus, Otfried, Koch, Hans Georg, Kurlemann, Gerhard, Sträter, Ronald, Vielhaber, Heinrich, Weber, Peter, Nowak-Göttl, Ulrike

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